U.S. patent application number 11/459717 was filed with the patent office on 2007-02-01 for fixing member with toner releasing layer, and fixing apparatus with the same.
This patent application is currently assigned to CANON KABUSHIKI KAISHA. Invention is credited to Yuji Kitano, Osamu Sotome.
Application Number | 20070025741 11/459717 |
Document ID | / |
Family ID | 37694427 |
Filed Date | 2007-02-01 |
United States Patent
Application |
20070025741 |
Kind Code |
A1 |
Kitano; Yuji ; et
al. |
February 1, 2007 |
FIXING MEMBER WITH TONER RELEASING LAYER, AND FIXING APPARATUS WITH
THE SAME
Abstract
A fixing member having a toner releasing layer superior in toner
releasability and a fixing apparatus provided with the fixing
member are provided. The toner releasing layer is composed of
fluororubber having an ether linkage in its molecule and a
polysiloxane-type surface-active agent having a polyether
structure.
Inventors: |
Kitano; Yuji; (Kawasaki-Shi,
JP) ; Sotome; Osamu; (Kawasaki-Shi, JP) |
Correspondence
Address: |
FITZPATRICK CELLA HARPER & SCINTO
30 ROCKEFELLER PLAZA
NEW YORK
NY
10112
US
|
Assignee: |
CANON KABUSHIKI KAISHA
TOKYO
JP
|
Family ID: |
37694427 |
Appl. No.: |
11/459717 |
Filed: |
July 25, 2006 |
Current U.S.
Class: |
399/1 |
Current CPC
Class: |
G03G 15/2057 20130101;
G03G 2215/2048 20130101 |
Class at
Publication: |
399/001 |
International
Class: |
G03G 15/00 20060101
G03G015/00 |
Foreign Application Data
Date |
Code |
Application Number |
Jul 29, 2005 |
JP |
2005-220624 |
Claims
1. A fixing member used in an electrophotographic image forming
apparatus, having a toner releasing layer formed on its surface,
wherein the toner releasing layer contains as a main component a
fluororubber having an ether linkage in its molecule, and further,
contains at least a polysiloxane-type surface-active agent having
at least a polyether structure.
2. The fixing member according to claim 1, wherein the toner
releasing layer has a sea-island structure in which the
fluororubber constitutes a sea phase and the polysiloxane-type
surface-active agent constitutes islands phases, and a number-based
average size of the island phases is 2 .mu.m or less.
3. The fixing member according to claim 1, wherein the fluororubber
is a terpolymer of vinylidene fluoride, tetrafluoroethylene and
perfluoromethyl vinyl ether.
4. The fixing member according to claim 1, wherein the
polysiloxane-type surface-active agent has a dimethylpolysiloxane
structure and a polyoxyalkylene structure.
5. The fixing member according to claim 1, wherein a blending
quantity of the polysiloxane-type surface-active agent is 20 to 60
parts by mass with respect to 100 parts by mass of the
fluororubber.
6. The fixing member according to claim 1, which is used as a
fixing roller, a fixing belt, a pressure roller or a pressure
belt.
7. The fixing member according to claim 1, which is used as a
fixing belt that is a single-layer fixing belt in which the toner
releasing layer has been formed on an outer peripheral surface of a
base material of the fixing belt, and a thickness of the toner
releasing layer is 60 to 150 .mu.m.
8. A fixing apparatus of an oilless system used in an
electrophotographic image forming apparatus, wherein the fixing
apparatus has a fixing member selected from the group consisting of
a fixing roller, a fixing belt, a pressure roller and a pressure
belt, and the fixing member is the fixing member according to claim
1.
9. The fixing apparatus according to claim 8, which is used for
fixing an unfixed image formed from a wax-containing toner.
Description
BACKGROUND OF THE INVENTION
[0001] 1. Field of the Invention
[0002] The present invention relates to a fixing member used for a
fixing apparatus in an electrophotographic image forming apparatus
such as a copier or an LBP, and in particular, relates to a fixing
member used preferably in a fixing apparatus of an oilless system.
In addition, the present invention relates to a fixing apparatus
using such a fixing member.
[0003] 2. Description of the Related Art
[0004] A fixing member is required to have high toner
releasability. If it has high toner releasability, when toner
images formed electrostatically on a recording material, such as
paper, is fixed with heat and pressure, it becomes hard for toner
to adhere on a surface of the fixing member. When toner adheres to
the member surface, that is, toner offset arises, a problem is
raised in that image quality deteriorates due to chips arising
partially in a toner image formed on a recording material, or
offset toner being re-fixed to the following recording material.
Hence, it has been investigated to use a material excellent in
toner releasability on the surface of a fixing member, that is, for
a releasing layer.
[0005] As such a fixing member, one is normally used in which a
layer structure composed of one or more layers is formed on the
outer periphery of a cylinder shaft, and a fluorocarbon resin is
used for a releasing layer.
[0006] Although the fluorocarbon resin has low surface energy and
is excellent in toner releasability, it has such a demerit that
material hardness is high, because it is a resin. If hardness is
high, when a toner image formed electrostatically is fixed with
heat and pressure, an ability to follow unevenness of paper fibers
is low, and hence, it becomes hard to obtain a high quality image.
In addition, on a recording material which hardly has
convexoconcave, it is difficult to obtain a high quality image
because toner particles are crushed more than needed and a small
character becomes illegible.
[0007] On the other hand, a member using a releasing layer
constructed of an elastic material has flexibility in comparison
with resins, and has such an advantage that it is easy to obtain a
high quality image. Nevertheless, as compared with the fluorocarbon
resin, an elastic material, that is, rubber, generally has high
surface energy, and is apt to be inferior in toner releasability.
In particular, only the fluorocarbon resin is put in practical use
as a material used for a releasing layer in color oilless fixing,
and a fixing member having a releasing layer constructed of rubber
has not been put in practical use up to now. In order to obtain a
high quality image, what is desired is not a releasing layer that
is constructed of a hard resin, but a releasing layer which is
constructed of a flexible rubber.
[0008] In addition, since a fixing member is used at a high
temperature of about 200.degree. C., a rubber used for a releasing
layer is required to have heat resistance. Generally, as types of
rubbers which have such heat resistance, fluororubber, silicone
rubber, etc. may be cited. Fluororubber refers to a type of rubber,
which is an elastic material, produced by adding a cross-linker, a
cross-linking assistant, a reinforcing compounding agent and the
like to a fluoropolymer which is constructed of partially
fluorinated hydrocarbon chains, and forming a three-dimensional
network through polyamine cross-linking, polyol cross-linking, or
organic peroxide cross-linking.
[0009] Heretofore, fluororubber has been used mainly as a releasing
layer in an oil coating system in which a denatured silicone oil is
externally supplied in a color machine. Types of fluororubber
polymers (fluoropolymers) are mainly used which are produced by
polyamine-cross-linking or polyol-cross-linking a product produced
by blending a metal-containing filler and a reinforcing bulking
agent with a fluoropolymer which is constructed of a binary
copolymer of vinylidene fluoride and hexafluoropropylene, or a
terpolymer of vinylidene fluoride, hexafluoropropylene and
tetrafluoroethylene.
[0010] Silicone rubber refers to a type of rubber, which is an
elastic material, produced by forming a three-dimensional network
through addition reaction cross-linking, organic peroxide
cross-linking or the like of a product produced by blending various
fillers as needed with a raw rubber such as polymers which are
constructed of methyl-vinyl siloxane units or methyl-phenyl-vinyl
siloxane units in which part of methyl groups of methyl-vinyl
siloxane units have been replaced by phenyl groups.
[0011] Generally, silicone rubber has been primarily used as a
thermally conductive elastic material lower layer because of
excellent heat resistance. In addition, as a releasing layer,
fluororubber has been mainly used in an oil coating system in which
dimethylsilicone oil is externally supplied in a color machine.
[0012] However, an oilless fixing system with a fluorocarbon resin
releasing layer has recently been put in practical use in which, in
order to secure releasability, a wax having a releasing assistant
effect is internally added to toner, and as mentioned above, no oil
coating is externally carried out.
[0013] When fluororubber is used for a releasing layer instead of a
fluorocarbon resin so as to obtain a high quality image, the
affinity between wax in toner and fluororubber was low, and the
releasing assistant effect of the wax is not fully exerted. Hence,
paper winding arising when toner does not come off a releasing
layer, or toner offset has occurred in some cases.
[0014] In addition, when dimethyl silicone rubber is used for a
releasing layer, the affinity between wax in toner and dimethyl
silicone rubber was high. But, the affinity is too high, and a
certain adverse effect is exerted on toner releasability, and thus,
paper winding or toner offset has occurred in some cases.
[0015] It is disclosed in Japanese Patent Application Laid-Open No.
2000-242115 to use a rubber releasing layer in color oilless
fixing. The above-mentioned document discloses an image recording
device in which a toner containing wax is used, and a releasing
layer constructed of fluororubber high in affinity with the wax is
formed on the fixing member surface on the side coming in contact
with an unfixed toner image on a recording material in a fixing
apparatus.
[0016] Although, in the above-mentioned document, the releasing
layer constructed of fluororubber high in affinity with wax is
proposed, this releasing layer is insufficient in toner
releasability, and further improvement in toner releasability is
desired.
[0017] In addition, Japanese Patent Application Laid-Open No.
2004-138956 proposes a fixing belt characterized in that a surface
layer is constructed of a vulcanization product of a liquid coating
composition having a ternary copolymer of tetrafluoroethylene,
vinylidene fluoride and hexafluoropropylene, a vulcanizing agent,
and silicone oil. It is described in this document that a silicone
oil is preferable which is partly substituted with a fluoro alkyl
group, or has at the end of its chemical structure a functional
group selected from among a hydroxyl group, an alkoxy group, a
carboxyl group and an alkoxy carbonyl group.
[0018] Although the above-mentioned document proposes the releasing
layer which is constructed of a mixture of general-purpose
fluororubber and silicone oil, it has no mention concerning the
dispersibility of fluororubber and silicone oil which are low in
affinity with each other. If a sea-island structure is taken when
the affinity between the two is low, the sizes of islands are
uneven. In the case where a particularly large island occurs, a
portion with insufficient toner releasability may arise.
SUMMARY OF THE INVENTION
[0019] An object of the present invention is to provide a fixing
member having a releasing layer constructed of an elastic material
which does not cause toner offset and is excellent in toner
releasability. More specifically, the present invention is to
provide a fixing member having a releasing layer in which the
dispersibility of a silicone compound into a fluororubber is
improved, and the silicone compound is finely dispersed in the
fluororubber.
[0020] Another object of the present invention is to provide a
fixing apparatus equipped with a fixing member which has such a
releasing layer.
[0021] The above-mentioned objects of the present invention are
achieved by the following invention.
[0022] The present invention relates to a fixing member used in an
electrophotographic image forming apparatus, having a toner
releasing layer formed on its surface, wherein the toner releasing
layer contains as a main component a fluororubber having an ether
linkage in its molecule, and further, contains at least a
polysiloxane-type surface-active agnet having at least a polyether
structure.
BRIEF DESCRIPTION OF THE DRAWINGS
[0023] FIG. 1 is a sectional view of a fixing member with a
single-layer structure.
[0024] FIG. 2 is a sectional view of a fixing member with a
two-layer structure.
[0025] FIG. 3 is a schematic structural diagram of one form of a
fixing apparatus.
[0026] FIG. 4 is a schematic structural diagram of a
belt-heating-type fixing apparatus.
DESCRIPTION OF THE EMBODIMENTS
[0027] As a means of suitably increasing the wax affinity of
fluororubber, it is conceivable to disperse polysiloxane (for
example, dimethylpolysiloxane) in the form of fine islands in the
fluororubber. It is possible to increase the affinity of
fluororubber with wax by dispersing polysiloxane high in affinity
with wax into fluororubber low in affinity with wax.
[0028] However, If dimethylpolysiloxane is simply mixed with
fluororubber, since the affinity between the two is low, the
dispersion state is coarse and dispersed grain sizes become
hundreds .mu.m in many cases. Accordingly, in the present
invention, the dispersibility of polysiloxane has been increased by
using a fluororubber having an ether linkage in its molecule, and
using as an additive a polysiloxane-type surface-active agent which
has a polyether structure and good affinity with the
fluoropolymer.
[0029] When dispersing the polysiloxane-type surface-active agent
in fluororubber as mentioned above, it is preferable to perform the
dispersion so as to create a sea-island structure in which the
fluororubber constitutes the sea phase and the polysiloxane-type
surface-active agent constitutes the island phases. In particular,
it is preferable to perform the dispersion so that the number-based
average size of the islands phases is 2 .mu.m or less, and more
preferably 0.1 .mu.m or more. It is possible to evenly increase the
releasability of toner from the surface of a fixing member by
finely dispersing a polysiloxane-type surface-active agent in
fluororubber.
[0030] The average sizes of the island phases can be measured by
electron microscope observation. Twenty island phases are selected
at random and the major axis of each of the island phases is
measured. An average value of fourteen measured values which are
obtained by removing three largest values and three smallest values
from the measured values is regarded as the average size.
[0031] The polysiloxane-type surface-active agent is a nonionic
surface-active agent which has preferably a dialkylpolysiloxane
structure and more preferably a dimethylpolysiloxane structure as a
hydrophobic group, and has preferably a polyether structure and
more preferably a polyoxyalkylene structure as a hydrophilic group.
Since the dialkyl polysiloxane-type surface-active agent has a
siloxane skeleton, it is low in volatility and excellent in thermal
stability, and hence, is suitable for a fixing member used at high
temperature.
[0032] As mentioned above, fluororubber polymers (fluoropolymers)
having been conventionally used include a binary copolymer of
vinylidene fluoride and hexafluoropropylene, and a ternary
copolymer of vinylidene fluoride, hexafluoropropylene, and
tetrafluoroethylene. Nevertheless, taking into account the affinity
with a polysiloxane-type surface-active agent having a polyether
structure, it is preferable to use fluororubber which has an ether
linkage. In particular, in the present invention, it is preferable
to use as the fluororubber a ternary copolymer of vinylidene
fluoride, tetrafluoroethylene and perfluoromethyl vinyl ether.
[0033] It is possible to classify the polysiloxane-type
surface-active agent used in the present invention into three types
of structures, taking dimethylpolysiloxane up as an example. That
is, they are a side-chain modification type constructed of a
structure in which polyoxyalkylene is bound to a side chain of a
dimethylpolysiloxane skeleton represented by the following formula
(1), a chain-end modification type which is constructed of a
structure in which polyoxyalkylene is bound to the chain end of a
dimethylpolysiloxane skeleton represented by the following formula
(2), and a copolymerization type which is constructed of a
structure in which dimethylpolysiloxane represented by the
following formula (3), and polyoxyalkylene are alternately bound
repeatedly. Among these, the copolymerization type represented by
the formula (3) is more preferable because its dispersibility into
fluororubber is most excellent. ##STR1##
[0034] (In the formulas, a and b each denote 0 or an integer, n and
m each denote an integer, and R and R' each denote a saturated
hydrocarbon group or an unsaturated hydrocarbon group.)
[0035] It is preferable that the blending quantity of the
polysiloxane-type surface-active agent is 20 to 60 parts by mass
(more preferably, 40 to 60 parts by mass) with respect to 100 parts
by mass of fluororubber. By using them within the above-described
range, the effect of improving the toner releasability can be
satisfactorily obtained, and it is possible to maintain the
mechanical strength of fluororubber within a satisfactory
range.
[0036] Although a cross-linker of fluororubber is not particularly
limited, since it is applicable also to publicly known polymers
with high fluorine contents and the durability of an elastomer
obtained becomes high, it is preferable to use an organic peroxide
cross-linker. Specifically, a polymer of fluororubber is of a type
in which iodine or bromine is introduced into the chain end or side
chain of its molecular chain, and the cross-linking by organic
peroxide is performed by an abstraction reaction of iodine or
bromine, and a radical reaction of a cross-linking assistant with
the allyl group.
[0037] Although the cross-linking is performed by heating after
forming a surface layer by solution coating, when the cross-linking
is performed using organic peroxide, hardening may be inhibited by
oxygen present in the air when atmospheric pressure hot air
cross-linking such as oven cross-linking is performed. Hence, in
order to cut off oxygen inhibiting hardening, it is preferable to
perform cross-linking by means of an oven whose inside atmosphere
has been replaced with nitrogen.
[0038] In view of surface energy, it is preferable that the rubber
(fluororubber) in the releasing layer does not contain various
fillers, for example, a reinforcing filler, or contains the fillers
in an amount of five or less parts by mass with respect to 100
parts by mass of a mixture of the fluororubber and
polysiloxane-type surface-active agent. If the releasing layer
contains more than five parts by mass of fillers, the toner
releasability may be lowered, which is not preferable.
[0039] The fixing member having a releasing layer constructed of
fluororubber can be produced as follows, for example. Fifty parts
by mass of polysiloxane-type surface-active agent having a
polyether structure, 4 parts by mass of triallyl isocyanurate as a
cross-linking assistant, and 3 parts by mass of benzoyl peroxide,
which is organic peroxide, as a cross-linker with respect to 100
parts by mass of fluoropolymer containing iodine or bromine as a
reaction group and an ether linkage in its molecule, are dissolved
in a ketone-type solvent, sufficiently stirred, then applied by
spray coating so as to form at least a surface layer of an elastic
material layer formed on the outer periphery of a roller or a belt
on which a primer has been uniformly applied and dried, and
thereafter, pass through a primary cross-linking step in an oven
whose inside atmosphere has been replaced with nitrogen and a
secondary cross-linking step in a normal heating oven, thereby
producing the fixing member.
[0040] Nevertheless, when a releasing layer is formed on thermally
conductive silicone rubber, a cross-linker and a cross-linking
assistant may migrate to the silicone rubber layer and their
amounts in the releasing layer may decrease. Hence, it is
preferable to beforehand blend the cross-linker and cross-linking
assistant in amounts several times as much as the above-mentioned
standard amounts. In addition, when a primer layer is formed on a
thermally conductive silicone rubber layer, what is publicly known
may be used as the primer layer, but it is preferable to use what
can prevent a cross-linker and a cross-linking assistant from
migrating. When using a publicly known primer, a thickness of the
primer layer is not limited particularly, but it is usually about 1
to 5 .mu.m.
[0041] FIG. 1 shows a cross-section of the fixing member having the
single-layer structure thus obtained. It may be a belt-like member
although FIG. 1 shows the structure of a roller. In FIG. 1,
reference numeral 1 denotes a roller base material, and reference
numeral 2 denotes a toner releasing layer which contains
fluororubber having an ether linkage in its molecule and a
polysiloxane-type surface-active agent having a polyether
structure.
[0042] The thickness of a toner releasing layer may be determined
suitably according to need, but, in order to secure sufficient flaw
and wear resistance, it is preferable that in general, the
thickness is 10 .mu.m or more. In addition, it is desirable that in
view of thermal conductivity, the thickness is 500 .mu.m or
less.
[0043] When used as a single-layer fixing belt with a toner
releasing layer superimposed on a base material, it is preferable
that the thickness of the toner releasing layer is 60 to 150 .mu.m.
If the thickness is brought into this range, it becomes possible to
suppress a sharp decline in thermal efficiency while imparting
elasticity to a belt surface.
[0044] In addition, the base material of a fixing belt is a
seamless belt of 10 to 50 .mu.m in thickness, and the material may
be selected from among heat resistant resins such as polyimide and
polyamidoimide, and metals such as SUS, nickel and aluminum. But,
the material made of a metal having a small electric resistance
value is preferable.
[0045] A fixing member with a two-layer structure is shown in FIG.
2. It may be a belt-like member although FIG. 2 shows the structure
of a roller. In the fixing member with a two-layer structure,
first, a thermally conductive elastic material layer 3 constructed
of conventional silicone rubber or the like is formed on the outer
periphery of the roller base material 1, and a releasing layer 2
which contains fluororubber having an ether linkage in its molecule
and a polysiloxane-type surface-active agent having a polyether
structure is formed on the outer periphery of the thermally
conductive elastic material layer 3.
[0046] As types of silicone rubbers used for a thermally conductive
elastic material layer, polydimethylsiloxane,
polymethylphenylsiloxane, etc. may be cited and it is preferable to
use one of these materials blended with a thermally conductive
filler. Such an elastic material layer may be formed by a
publicly-known method such as a method in which a silicone rubber
is injected into a molding die and heat-cured or a method in which
a silicone polymer layer is formed through coating and cured by
means of a heating oven.
[0047] It is preferable that the thickness of the thermally
conductive elastic material layer is 50 .mu.m or more in order to
secure properties of following a recording material such as paper
and is 5 mm or less in respect of the thermal conductivity.
[0048] Also in this case, the thickness of a releasing layer may be
determined as in the case of a fixing member having a single-layer
structure and the preferable range is 10 to 500 .mu.m.
[0049] The fixing member of the present invention is not restricted
to the above fixing member having a single-layer or two-layer
structure and may have a multilayer structure composed of three
layers or more, and besides, may be in the form of a fixing belt, a
fixing roller, a pressure belt or a pressure roller.
[0050] It is preferable that the toner releasing layer is
10.degree. to 60.degree. in rubber hardness defined in JIS-A. In
this case, images having higher quality can be obtained.
[0051] Next, a fixing apparatus of the present invention is
described. The fixing apparatus of the present invention is used in
an electrophotographic image forming apparatus and has a fixing
member selected from the group consisting of a fixing roller, a
fixing belt, a pressure roller and a pressure belt. The above
fixing member is used as the fixing member. The electrophotographic
image forming apparatus has, besides the fixing apparatus, a
photosensitive member, a latent image forming means, a means for
developing the formed latent image with toner and a means for
transferring the developed toner image to a transfer material.
[0052] FIG. 3 shows a structural diagram of a fixing apparatus of
the present invention. A fixing roller 4 as a upper roller and a
pressure roller 5 as a lower roller are set in the fixing
apparatus. A fixing member of the present invention is used for the
fixing roller 4 and pressure roller 5. A heater 6 constituted of a
halogen lamp is installed in each of the center of the fixing
roller 4 and the center of the pressure roller 5.
[0053] The fixing roller 4 is rotated in the direction of an arrow
at a predetermined speed and the pressure roller 5 is also rotated
in the direction of an arrow in accordance with the fixing roller
4. Then, a toner image formed on a recording material such as paper
is fixed by heat from the heater 6 and the pressure applied between
the fixing roller 4 and the pressure roller 5.
[0054] The fixing temperature is kept at a set temperature by
controlling an output of the heater 6 in accordance with the
surface temperature of the fixing roller 4 measured by a thermistor
7. Though the surface temperature (fixing temperature) of the
fixing roller 4 is not particularly restricted, it normally ranges
from 130.degree. to 220.degree. C.
[0055] A fixing apparatus using a upper roller and a lower roller
is taken up herein as an example. However, a fixing apparatus of
the present invention may have a fixing member of the present
invention as a fixing belt, a fixing roller, a pressure belt or a
pressure roller and is not restricted to the fixing apparatus shown
in FIG. 3.
[0056] Next, a belt-heating-type fixing apparatus using a robber
single-layer fixing belt is described with reference to FIG. 4.
[0057] In FIG. 4, reference numeral 8 denotes an endless-belt-like
rubber single-layer fixing, reference numeral 11 denotes a belt
guide portion, and reference numeral 12 denotes a stay. Reference
numeral 9 denotes a heating member having a layer formed by
applying an electric resistance material such as silver palladium
(Ag/Pd) which generates heat by allowing an electric current to
flow therethrough, on a heating substrate made of alumina or
ceramic by screen printing in the form of lines or belts. Besides,
a glass coating layer of about 10 .mu.m in thickness is formed on
the layer to protect the electric resistance material and to secure
insulating properties. Furthermore, a thermistor is in contact with
the back side of the heating substrate. Therefore, it is possible
to keep the surface temperature of the rubber single-layer fixing
belt at a temperature capable of fixing by controlling the power
applied to the electric resistance material in accordance with the
temperature detected by the thermistor.
[0058] Reference numeral 10 denotes a pressure roller which is one
conformation of a pressure member. An elastic material layer made
of silicone rubber having a thickness of 1 to 5 mm is formed on a
mandrel made of aluminum, and on this elastic material layer, a
releasing layer may be formed which is composed of a fluorocarbon
resin such as PFA, FEP or PTFE having a thickness of 10 to 50
.mu.m. The pressure roller is brought into pressure-contact with a
heating body through a rubber single-layer fixing belt and rotated
by a pressure roller driving means. The pressure roller 5 is
rotated and the rubber single-layer fixing belt 8 is rotated
following the rotation of the roller 5. A recording material such
as paper with an unfixed image formed thereon is held and conveyed
between the rubber single-layer fixing belt 8 and the pressure
roller 10, whereby the unfixed image is heated and fixed to the
recording material.
[0059] The present invention will be described below in detail by
giving examples. However, the present invention is by no means
limited to them.
EXAMPLES
Example 1
[0060] A weight of 100 g of fluoropolymer (trade name: DAIERU LT302
made by DAIKIN INDUSTRIES, LTD.) composed of a ternary copolymer of
vinylidene fluoride containing iodine as a reactive radical in its
molecule, tetrafluoroethylene and perfluoromethyl vinyl ether, 40 g
of a copolymerization type of polysiloxane-type surface-active
agent having a structure in which dimethylpolysiloxane and
polyoxialkylene had been alternately repetitively combined (trade
name: FZ-2207 made by TORAY Dow Corning Co., Ltd.), 4 g of triallyl
isocyanurate (trade name: TAIC made by Nippon Kasei Chemical Co.,
Ltd.) as a cross-linking assistant and 4 g of benzoyl peroxide (an
organic peroxide) as a cross-linking agent (water content: 25%;
made by KISHIDA KAGAKU Co., Ltd.) were dissolved in 900 g of methyl
isobutyl ketone (a ketone-type solvent), to thereby prepare a
coating solution.
[0061] A thermally conductive elastic material layer made of
silicone rubber having a thickness of 1.5 mm was formed on the
surface of a roller having an outside diameter of 35 mm and a
primer (trade name: MEGUM3290 made by Chemetall Inc.) was uniformly
applied on the surface of the layer to have a thickness of 2 .mu.m
and dried. The coating solution prepared above was sufficiently
stirred and applied by spray-coating on the outer periphery of the
roller to have a thickness of 30 .mu.m after dyied. Then, the
coated roller was heated in an oven whose inside atmosphere had
been replaced with nitrogen at 200.degree. C., thereby performing
primary cross-linking, and secondary cross-linking was carried out
(at 180.degree. for 24 hr) in a normal oven. Thus, a fixing member
in which a releasing layer was superimposed on the thermally
conductive elastic material layer was produced.
[0062] In addition, a sample for analyzing the releasing layer was
prepared to examine the dispersive conformation of the
polysiloxane-type surface-active agent in the cross section of the
sample. As a result, it was found that the sample had a sea-island
structure in which the fluororubber constituted a sea phase and the
polysiloxane-type surface-active agent constituted island phases
and the number-based average size of the island phases was 0.8
.mu.m.
[0063] In addition, a fluororubber layer 10 mm in thickness having
the same formulation as the releasing layer was formed on a flat
plate, and the rubber harness of the fluororubber layer thus formed
was measured. As a result, the rubber hardness was 32.degree..
[0064] The fixing member produced by the above method is set in a
fixing apparatus having the configuration shown in FIG. 3 as the
fixing roller 4. Transfer sheets holding unfixed images formed from
a wax-containing toner were fed to the fixing apparatus. The
unfixed images of the wax-contained toner were formed by using a
color printer LBP-5900 manufactured by CANON INC. from which a
fixing apparatus had been removed. The transfer sheets holding the
unfixed images were fed under the condition that the surface
temperature on the fixing side of the fixing means was set at
180.degree. C. and a process speed was 90 mm/sec., and such an
evaluation as described later was made.
Example 2
[0065] A fixing member was produced in the same manner as in
Example 1 except that the blending quantity of the copolymerization
type of polysiloxane-type surface-active agent (trade name: FZ-2207
made by TORAY Dow Corning Co., Ltd.) was changed to 20 g. Transfer
sheets holding unfixed images formed from a wax-containing toner
were fed in the same manner as in Example 1 except that the fixing
member was used as the fixing roller 4, and the same evaluation as
in Example 1 was made.
[0066] In addition, a sample for analyzing the releasing layer was
prepared to examine the dispersive conformation of the
polysiloxane-type surface-active agent in the cross section of the
sample. As a result, it was found that the sample had a sea-island
structure in which the fluororubber constituted a sea phase and the
polysiloxane-type surface-active agent constituted island phases
and the number-based average size of the island phases was 0.7
.mu.m.
[0067] The rubber hardness of the releasing layer was measured in
the same manner as in Example 1, and found to be 40.degree..
Example 3
[0068] A fixing member was produced in the same manner as in
Example 1 except that the blending quantity of the copolymerization
type of polysiloxane-type surface-active agent (trade name: FZ-2207
made by TORAY Dow Corning Co., Ltd.) was changed to 60 g. Transfer
sheets holding unfixed images formed from a wax-containing toner
were fed in the same manner as in Example 1 except that the fixing
member was used as the fixing roller 4, and the same evaluation as
in Example 1 was made.
[0069] In addition, a sample for analyzing the releasing layer was
prepared to examine the dispersive conformation of the
polysiloxane-type surface-active agent in the cross section of the
sample. As a result, it was found that the sample had a sea-island
structure in which the fluororubber constituted a sea phase and the
polysiloxane-type surface-active agent constituted island phases
and the number-based average size of the island phases was 0.9
.mu.m.
[0070] The rubber hardness of the releasing layer was measured in
the same manner as in Example 1, and found to be 29.degree..
Example 4
[0071] A fixing member was produced in the same manner as in
Example 1 except that the polysiloxane-type surface-active agent
was changed to a side-chain modification type constituted of a
structure in which polyoxyalkylene was combined with a side-chain
of a dimethlypolysiloxane skeleton (trade name: FZ-5609 made by
TORAY Dow Corning Co., Ltd.).
[0072] Transfer sheets holding unfixed images formed from a
wax-containing toner was fed in the same manner as in Example 1
except that the fixing member was used as the fixing roller 4, and
the same evaluation as in Example 1 was made.
[0073] In addition, a sample for analyzing the releasing layer was
prepared to examine the dispersive conformation in the cross
section of the sample. As a result, it was found that the sample
had a sea-island structure in which the fluororubber constituted a
sea phase and the polysiloxane-type surface-active agent
constituted island phases and the number-based average size of the
island phases was 2 .mu.m.
[0074] The rubber hardness of the releasing layer was measured in
the same manner as in Example 1, and found to be 33.degree..
Example 5
[0075] A fixing member was produced in the same manner as in
Example 1 except that the polysiloxane-type surface-active agent
was changed to a chain-end modification type (trade name: L-720
made by TORAY Dow Corning Co., Ltd.) constituted of a structure in
which polyoxyalkylene was combined with the chain end of a
dimethlypolysiloxane skeleton (trade name: L-720 made by TORAY Dow
Corning Co., Ltd.).
[0076] Transfer sheets holding unfixed images formed from a
wax-containing toner were fed in the same manner as in Example 1
except that the fixing member was used as the fixing roller 4, and
the same evaluation as in Example 1 was made.
[0077] In addition, a sample for analyzing the releasing layer was
prepared to examine the dispersive conformation of the
polysiloxane-type surface-active agent in the cross section of the
sample. As a result, it was found that the sample had a sea-island
structure in which the fluororubber constituted a sea phase and the
polysiloxane-type surface-active agent constituted island phases
and the number-based average size of the island phases was 2
.mu.m.
[0078] The rubber hardness of the releasing layer was measured in
the same manner as in Example 1, and found to be 33.degree..
Comparative Example 1
[0079] A fixing member was produced in the same manner as in
Example 1 except that the fluoropolymer used in Example 1 was
changed to fluoropolymer (trade name: DAIERU G902 made by DAIKIN
INDUSTRIES, LTD.) composed of a ternary copolymer of vinylidene
fluroride containing iodine as a reactive group in its molecule,
hexafluoropropylene and tetrafluoroethylene.
[0080] Transfer sheets holding unfixed images formed from a
wax-contained toner were fed in the same manner as in Example 1
except that the fixing member produced by the above method was used
as the fixing roller 4, and the same evaluation as in Example 1 was
made.
[0081] In addition, a sample for analyzing the releasing layer was
prepared to examine the dispersive conformation of the
polysiloxane-type surface-active agent in the surface and the cross
section of the sample. As a result, the cross section of the sample
had a sea-island structure in which the fluororubber constituted a
sea phase and the polysiloxane-type surface-active agent
constituted island phases, but only the fluororubber was present on
the surface and the number-based average size of the island phases
in the cross section was 30 .mu.m.
[0082] The rubber hardness of the releasing layer was measured in
the same manner as in Example 1, and found to be 34.degree..
Comparative Example 2
[0083] A fixing member was produced in the same manner as in
Example 1 except that dimethylpolysiloxane was blended instead of
the polysiloxane-type surface-active agent and the bending quantity
of benzoyl peroxide serving as a cross-linking agent was changed to
5.6 g.
[0084] Transfer sheets holding unfixed images formed from a
wax-containing toner were fed in the same manner as in Example 1
except that the fixing member prepared by the above method was used
as the fixing roller 4, and the same evaluation as in Example 1 was
made.
[0085] In addition, a sample for analyzing the releasing layer was
prepared to examine the dispersive conformation of the
polysiloxane-type surface-active agent in the surface and the cross
section of the sample. As a result, it was found that the cross
section had a sea-island structure in which the fluororubber
constituted a sea phase and the dimethylpolysiloxane constituted
island phases, but only the fluororubber was present on the surface
and the number-based average size of the island phases in the cross
section was 50 .mu.m.
[0086] The rubber hardness of the releasing layer was measured in
the same manner as in Example 1, and found to be 34.degree..
[0087] Table 1 shows the formulations and evaluation results in
Examples 1 to 5 and Comparative Examples 1 and 2. TABLE-US-00001
TABLE 1 Dispersive Rubber Blending conformation of hardness Type of
quantity polysiloxane- of fluororubber Type of compounding (parts
type surface- releasing toner polymer agent by mass) active agent
layer (.degree.) releasability Ex. 1 VDF-TFE- Copolymerization 40
Island phase of 32 A PMVE type of polysiloxane- 0.8 .mu.m ype
surface-active agent Ex. 2 VDF-TFE- Copolymerization type 20 Island
phase of 40 A PMVE of polysiloxane-type 0.7 .mu.m surface-active
agent Ex. 3 VDF-TFE- Copolymerization type 60 Island phase of 29 A
PMVE of polysiloxane-type 0.9 .mu.m surface-active agent Ex. 4
VDF-TFE- Side-chain 40 Island phase of 33 B PMVE modification type
of 2 .mu.m polysiloxane-type surface-active agent Ex. 5 VDF-TFE-
Chain-end modification 40 Island phase of 33 B PMVE type of
polysiloxane- 2 .mu.m type surface-active agent Com. VDF-HFP-
Copolymerization type 40 Island phase of 34 D Ex. 1 TFE of
polysiloxane-type 30 .mu.m surface-active agent Com. VDF-TFE-
Dimethyl-polysiloxane 40 Island phase of 34 C Ex. 2 PMVE 50 .mu.m
Type of fluororubber polymer VDF: Vinylidenefluoride, HFP:
Hexafluoropropylene TFE: Tetrafluoroethylene, PMVE: Perfluoromethyl
vinyl ether
[0088] Toner releasability was evaluated in accordance with the
following references. [0089] A: Offset does not occur after feeding
30,000 sheets. [0090] B: Offset does not occur after feeding 20,000
sheets. [0091] C: Offset occurs at the 100-th sheet. [0092] D:
Offset occurs from the first sheet.
[0093] In Examples 1 and 3, the fixing rollers were used having a
releasing layer in which a ternary copolymer of vinylidenefluoride
having an ether linkage in its molecule, tetrafluoroethylene and
perfluoromethyl vinyl ether was used as a type of fluororubber
polymer and a copolymerization type of polysiloxane-type surface
active agent having a polyether structure was blended. As a result
of feeding transfer sheets holding unfixed images formed from a
wax-containing toner, the toner releasability was good, and even at
the time 30,000 sheets had been fed, a blank area created by offset
was not observed on the fixed images and high quality toner images
were obtained.
[0094] In Example 2 in which the blending quantity of the
polysiloxane-type surface-active agent is 20 parts by weight, as a
result of feeding transfer sheets holding unfixed images formed
from a wax-containing toner, the toner releasability was is good.
At the time 20,000 sheets had been fed, an blank area created by
offset was not observed on fixed images and high-quality toner
images were obtained.
[0095] In Example 4, the polysiloxane-type surface-active agent
used in Example 1 was changed to a side chain modification type of
polysiloxane-type surface-active agent having a polyether
structure, and in Example 5, to a chain-end modification type of
polysiloxane-type surface-active agent having a polyether
structure. In the evaluation made by using the fixing rollers
produced in Examples 4 and 5, the toner releasability was good, and
at the time 20,000 sheets had been fed, a blank area created by
offset was not observed on fixed images and high-quality toner
images were obtained.
[0096] In Comparative Example 1, a copolymerization type of
polysiloxane-type surface-active agent having a polyether structure
was blended, but a ternary copolymer of vinylidene fluoride having
no ether linkage in its molecule, hexafluoropropylene and
tetrafluoroethylene was used as a type of fluororubber polymer. In
this case, the dispersive conformation of the polysiloxane
surface-active agent was rough. As a result of feeding transfer
sheets holding unfixed images formed from a wax-containing toner,
the toner releasability was insufficient, and at the time the first
sheet was fed, a blank area created by offset occurred on fixed
images and the fixing performance was unsatisfactory.
[0097] In Comparative Example 2, fluorine rubber having an ether
linkage in its molecule was used, but dimethylpolysiloxane having
no alkylene oxide was blended. In this case, the dispersive
conformation of the polysiloxane-type surface-active agent was
rough. As a result of feeding transfer sheets holding unfixed
images formed from a wax-containing toner, and the toner
releasability was insufficient, and at the time the 100-th sheet
was fed, offset occurred and the fixing performance was
unsatisfactory.
Example 6
[0098] A weight of 100 g of fluoropolymer composed of a ternary
copolymer of vinylidene fluoride having iodine as a reactive group
in its molecule, tetrafluoroethylene and perfluoromethyl vinyl
ether (trade name: DAIERU LT302 made by DAIKIN INDUSTRIES, LTD.),
50 g of a copolymerization type of polysiloxane-type surface-active
agent having a structure in which dimethylpolysiloxane and
polyoxialkylene had alternately repeatedly been combined (trade
name: FZ-2207 made by TORAY Dow Corning Co., Ltd.), 4 g of triallyl
isocyanurate (trade name: TAIC made by Nippon Kasei Chemical Co.,
Ltd.) as a cross-linking assistant and 4 g of benzoyl peroxide (an
organic peroxide) as a cross-linking agent (water content: 25%,
made by KISHIDA KAGAKU Co., Ltd.) were dissolved in 900 g of methyl
isobutyl ketone (a ketone-type solvent), thereby preparing a
coating solution.
[0099] A primer (trade name: MEGUM3290 made by Chemetall Inc.) was
uniformly applied on the surface of a belt base material (made of
SUS; outside diameter: 30 mm; thickness: 30 .mu.m) and dried. The
coating solution prepared above was applied by spray-coating on the
outer periphery of the belt to have a thickness of 100 .mu.m. Then,
the coated roller was heated in an oven whose inside atmosphere had
been replaced with nitrogen at 130.degree. C. for 1 hr, thereby
performing primary cross-linking, and secondary cross-linking was
carried out in a normal oven at 180.degree. C. for 24 hr. Thus, a
single-layer fixing belt having a releasing layer on the base
material was produced.
[0100] The single-layer fixing belt produced by the above method
was set in a belt-heating-type fixing apparatus having the
structure shown in FIG. 4 as the fixing belt 8. Transfer sheets
holding unfixed images formed from a wax-containing toner was fed
to the fixing apparatus. The unfixed full-color images of the
wax-containing toner were formed by using a color printer LBP-5900
made by CANON INC. from which a fixing apparatus had been removed.
The transfer sheets holding the unfixed images were fed under the
condition that the surface of the single-layer fixing belt was set
at 180.degree. C. and a process speed was 90 mm/sec, and the fixed
images were visually evaluated.
[0101] In addition, the electric resistance value in the
cross-sectional direction of the rubber single-layer fixing belt
was measured. In the case of the electric resistance value was a
value measured when applying a voltage of 400 V at an area of 11.9
cm.sup.2 in the belt cross-sectional direction. The electric
resistance value thus measured was 1.times.10.sup.9 .OMEGA..
[0102] The heat transfer properties of the rubber single-layer
fixing belt was evaluated according to the paper-surface ultimate
temperature reached when a sheet of paper with a thermocouple
attached thereto was fed in the steady state in which the surface
temperature of the rubber single-layer fixing belt was 180.degree.
C. The temperature thus measured was 142.degree. C.
[0103] Furthermore, the rubber hardness of the releasing layer
similarly was measured in the same manner as in Example 1, and
found to be 30.degree..
Example 7
[0104] A single-layer fixing belt was produced in the same manner
as in Example 6 except that the thickness of the releasing layer
(rubber layer) was set to 60 .mu.m. Transfer sheets holding unfixed
full-color images formed from a wax-containing toner were fed in
the same manner as in Example 6 except that the single-layer fixing
belt prepared by the above method was used as the fixing belt 8,
and the fixed images were visually evaluated.
[0105] The electric resistance value in the cross-sectional
direction of the rubber single-layer fixing belt was measured in
the same manner as in Example 6, and found to be 5.times.10.sup.8
.OMEGA..
[0106] In addition, the paper-surface ultimate temperature was
measured in the same manner as in Example 6, and found to be
148.degree. C.
[0107] Furthermore, the rubber hardness of the mold release layer
was measured in the same manner as in Example 1, and found to be
30.degree..
Example 8
[0108] A single-layer fixing belt was produced in the same manner
as in Example 6 except that the thickness of the release layer
(rubber layer) was set to 150 .mu.m. Transfer sheets holding
unfixed full-color image formed from a wax-containing toner were
fed in the same manner as in Example 6 except that the single-layer
fixing belt prepared by the above method was used as the fixing
belt 8, and the fixed images were visually evaluated.
[0109] The electric resistance value in the cross-sectional
direction of the above rubber single-layer fixing belt waa measured
in the same manner as in Example 6, and found to be
2.times.10.sup.9 .OMEGA..
[0110] In addition, the paper-surface ultimate temperature was
measured in the same manner as in Example 6, and found to be
135.degree. C.
[0111] Furthermore, the rubber hardness of the releasing layer was
measured in the same manner as in Example 1, and found to be
30.degree..
[0112] Table 2 shows the formulations and evaluation results in
Examples 6 to 8. The evaluation references of toner releasability
were the same as the evaluation references in Example 1.
TABLE-US-00002 TABLE 2 Dispersive Rubber conformation hardness
Blending of of Type of quantity polysiloxane releasing Fluororubber
Type of (parts by surface- layer Toner polymer compounding agent
mass) active agent (.degree.) releasability Ex. 6 VDF-
Copolymerization 50 Island phase 30 A TFE- type of of 0.8 .mu.m
PMVE polysiloxane-type surface-active agent Ex. 7 VDF-
Copolymerization 50 Island phase 30 A TFE- type of of 0.8 .mu.m
PMVE polysiloxane-type surface-active agent Ex. 8 VDF-
Copolymerization 50 Island phase 30 A TFE- type of of 0.8 .mu.m
PMVE polysiloxane-type surface-active agent Type of fluororubber
polymer VDF: Vinylidenefluoride, HFP: Hexafluoropropylene TFE:
Tetrafluoroethylene, PMVE: Perfluoromethyl vinyl ether
[0113] While the present invention has been described with
reference to exemplary embodiments, it is to be understood that the
invention is not limited to the disclosed exemplary embodiments.
The scope of the following claims is to be accorded the broadest
interpretation so as to encompass all such modifications and
equivalent structures and functions.
[0114] This application claims the benefit of Japanese Patent
Application No. 2005-220624, filed Jul. 29, 2005, which is hereby
incorporated by reference herein in its entirety.
* * * * *